Proteases, proteolysis and inflammatory molecules in the tears of people with keratoconus

. Purpose:  To investigate the expression of proteases, proteolytic activity and cytokines in the tear film of people with keratoconus. Methods:  Basal tears from people with keratoconus, from individuals who had undergone corneal collagen cross‐linking for the treatment of keratoconus, and from nor...

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Published inActa ophthalmologica (Oxford, England) Vol. 90; no. 4; pp. e303 - e309
Main Authors Balasubramanian, Sivaraman Arumugam, Mohan, Sujatha, Pye, David Cecil, Willcox, Mark Duncan Perry
Format Journal Article
LanguageEnglish
Published Oxford, UK Blackwell Publishing Ltd 01.06.2012
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Abstract . Purpose:  To investigate the expression of proteases, proteolytic activity and cytokines in the tear film of people with keratoconus. Methods:  Basal tears from people with keratoconus, from individuals who had undergone corneal collagen cross‐linking for the treatment of keratoconus, and from normal controls were collected using a capillary tube. Corneal curvature of each subject was mapped. The total protein in tears was estimated. Levels and activity of proteases in the tears were analysed using specific antibody arrays and activity assays. Results:  The total tear protein level was significantly reduced in keratoconus (4.1 ± 0.9 mg/ml) compared with normals (6.7 ± 1.4 mg/ml) (p < 0.0001) or subjects who had undergone corneal collagen cross‐linking (5.7 ± 2.3 mg/ml) (p < 0.005). Significantly (p < 0.05) increased tear expression of matrix metalloproteinases (MMP) ‐1, ‐3, ‐7, ‐13, interleukins (IL) ‐4, ‐5, ‐6, ‐8 and tumour necrosis factor (TNF) ‐α, ‐β were evident in keratoconus. Tear IL‐6 was the only cytokine significantly (p < 0.05) increased in tears of keratoconus subjects compared with the collagen cross‐linked group. No significant difference in tear proteases were observed between the normal and the cross‐linked groups, although the expression of TNF‐α was significantly (p < 0.05) increased in the cross‐linked group compared with the controls. Elevated gelatinolytic (87.5 ± 33.6 versus 45.8 ± 24.6 FIU, p < 0.0001) and collagenolytic (6.1 ± 3.2 versus 3.6 ± 2.0 FIU, p < 0.05) activities were observed in tears from keratoconus compared with normal subjects. The activity of tear gelatinases (69.6 ± 22.2 FIU) and collagenases (5.7 ± 3.3 FIU) in the collagen cross‐linked group was not significantly different compared with either keratoconus or normals. Conclusion:  Tears of people with keratoconus had 1.9 times higher levels of proteolytic activity and over expression of several MMPs and cytokines compared with tears from controls. Further investigations are required to study the possible implications of these changes and whether they can be used to monitor disease progression or determine the success of corneal collagen cross‐linking.
AbstractList . Purpose:  To investigate the expression of proteases, proteolytic activity and cytokines in the tear film of people with keratoconus. Methods:  Basal tears from people with keratoconus, from individuals who had undergone corneal collagen cross‐linking for the treatment of keratoconus, and from normal controls were collected using a capillary tube. Corneal curvature of each subject was mapped. The total protein in tears was estimated. Levels and activity of proteases in the tears were analysed using specific antibody arrays and activity assays. Results:  The total tear protein level was significantly reduced in keratoconus (4.1 ± 0.9 mg/ml) compared with normals (6.7 ± 1.4 mg/ml) (p < 0.0001) or subjects who had undergone corneal collagen cross‐linking (5.7 ± 2.3 mg/ml) (p < 0.005). Significantly (p < 0.05) increased tear expression of matrix metalloproteinases (MMP) ‐1, ‐3, ‐7, ‐13, interleukins (IL) ‐4, ‐5, ‐6, ‐8 and tumour necrosis factor (TNF) ‐α, ‐β were evident in keratoconus. Tear IL‐6 was the only cytokine significantly (p < 0.05) increased in tears of keratoconus subjects compared with the collagen cross‐linked group. No significant difference in tear proteases were observed between the normal and the cross‐linked groups, although the expression of TNF‐α was significantly (p < 0.05) increased in the cross‐linked group compared with the controls. Elevated gelatinolytic (87.5 ± 33.6 versus 45.8 ± 24.6 FIU, p < 0.0001) and collagenolytic (6.1 ± 3.2 versus 3.6 ± 2.0 FIU, p < 0.05) activities were observed in tears from keratoconus compared with normal subjects. The activity of tear gelatinases (69.6 ± 22.2 FIU) and collagenases (5.7 ± 3.3 FIU) in the collagen cross‐linked group was not significantly different compared with either keratoconus or normals. Conclusion:  Tears of people with keratoconus had 1.9 times higher levels of proteolytic activity and over expression of several MMPs and cytokines compared with tears from controls. Further investigations are required to study the possible implications of these changes and whether they can be used to monitor disease progression or determine the success of corneal collagen cross‐linking.
To investigate the expression of proteases, proteolytic activity and cytokines in the tear film of people with keratoconus. Basal tears from people with keratoconus, from individuals who had undergone corneal collagen cross-linking for the treatment of keratoconus, and from normal controls were collected using a capillary tube. Corneal curvature of each subject was mapped. The total protein in tears was estimated. Levels and activity of proteases in the tears were analysed using specific antibody arrays and activity assays. The total tear protein level was significantly reduced in keratoconus (4.1 ± 0.9 mg/ml) compared with normals (6.7 ± 1.4 mg/ml) (p < 0.0001) or subjects who had undergone corneal collagen cross-linking (5.7 ± 2.3 mg/ml) (p < 0.005). Significantly (p < 0.05) increased tear expression of matrix metalloproteinases (MMP) -1, -3, -7, -13, interleukins (IL) -4, -5, -6, -8 and tumour necrosis factor (TNF) -α, -β were evident in keratoconus. Tear IL-6 was the only cytokine significantly (p < 0.05) increased in tears of keratoconus subjects compared with the collagen cross-linked group. No significant difference in tear proteases were observed between the normal and the cross-linked groups, although the expression of TNF-α was significantly (p < 0.05) increased in the cross-linked group compared with the controls. Elevated gelatinolytic (87.5 ± 33.6 versus 45.8 ± 24.6 FIU, p < 0.0001) and collagenolytic (6.1 ± 3.2 versus 3.6 ± 2.0 FIU, p < 0.05) activities were observed in tears from keratoconus compared with normal subjects. The activity of tear gelatinases (69.6 ± 22.2 FIU) and collagenases (5.7 ± 3.3 FIU) in the collagen cross-linked group was not significantly different compared with either keratoconus or normals. Tears of people with keratoconus had 1.9 times higher levels of proteolytic activity and over expression of several MMPs and cytokines compared with tears from controls. Further investigations are required to study the possible implications of these changes and whether they can be used to monitor disease progression or determine the success of corneal collagen cross-linking.
To investigate the expression of proteases, proteolytic activity and cytokines in the tear film of people with keratoconus.PURPOSETo investigate the expression of proteases, proteolytic activity and cytokines in the tear film of people with keratoconus.Basal tears from people with keratoconus, from individuals who had undergone corneal collagen cross-linking for the treatment of keratoconus, and from normal controls were collected using a capillary tube. Corneal curvature of each subject was mapped. The total protein in tears was estimated. Levels and activity of proteases in the tears were analysed using specific antibody arrays and activity assays.METHODSBasal tears from people with keratoconus, from individuals who had undergone corneal collagen cross-linking for the treatment of keratoconus, and from normal controls were collected using a capillary tube. Corneal curvature of each subject was mapped. The total protein in tears was estimated. Levels and activity of proteases in the tears were analysed using specific antibody arrays and activity assays.The total tear protein level was significantly reduced in keratoconus (4.1 ± 0.9 mg/ml) compared with normals (6.7 ± 1.4 mg/ml) (p < 0.0001) or subjects who had undergone corneal collagen cross-linking (5.7 ± 2.3 mg/ml) (p < 0.005). Significantly (p < 0.05) increased tear expression of matrix metalloproteinases (MMP) -1, -3, -7, -13, interleukins (IL) -4, -5, -6, -8 and tumour necrosis factor (TNF) -α, -β were evident in keratoconus. Tear IL-6 was the only cytokine significantly (p < 0.05) increased in tears of keratoconus subjects compared with the collagen cross-linked group. No significant difference in tear proteases were observed between the normal and the cross-linked groups, although the expression of TNF-α was significantly (p < 0.05) increased in the cross-linked group compared with the controls. Elevated gelatinolytic (87.5 ± 33.6 versus 45.8 ± 24.6 FIU, p < 0.0001) and collagenolytic (6.1 ± 3.2 versus 3.6 ± 2.0 FIU, p < 0.05) activities were observed in tears from keratoconus compared with normal subjects. The activity of tear gelatinases (69.6 ± 22.2 FIU) and collagenases (5.7 ± 3.3 FIU) in the collagen cross-linked group was not significantly different compared with either keratoconus or normals.RESULTSThe total tear protein level was significantly reduced in keratoconus (4.1 ± 0.9 mg/ml) compared with normals (6.7 ± 1.4 mg/ml) (p < 0.0001) or subjects who had undergone corneal collagen cross-linking (5.7 ± 2.3 mg/ml) (p < 0.005). Significantly (p < 0.05) increased tear expression of matrix metalloproteinases (MMP) -1, -3, -7, -13, interleukins (IL) -4, -5, -6, -8 and tumour necrosis factor (TNF) -α, -β were evident in keratoconus. Tear IL-6 was the only cytokine significantly (p < 0.05) increased in tears of keratoconus subjects compared with the collagen cross-linked group. No significant difference in tear proteases were observed between the normal and the cross-linked groups, although the expression of TNF-α was significantly (p < 0.05) increased in the cross-linked group compared with the controls. Elevated gelatinolytic (87.5 ± 33.6 versus 45.8 ± 24.6 FIU, p < 0.0001) and collagenolytic (6.1 ± 3.2 versus 3.6 ± 2.0 FIU, p < 0.05) activities were observed in tears from keratoconus compared with normal subjects. The activity of tear gelatinases (69.6 ± 22.2 FIU) and collagenases (5.7 ± 3.3 FIU) in the collagen cross-linked group was not significantly different compared with either keratoconus or normals.Tears of people with keratoconus had 1.9 times higher levels of proteolytic activity and over expression of several MMPs and cytokines compared with tears from controls. Further investigations are required to study the possible implications of these changes and whether they can be used to monitor disease progression or determine the success of corneal collagen cross-linking.CONCLUSIONTears of people with keratoconus had 1.9 times higher levels of proteolytic activity and over expression of several MMPs and cytokines compared with tears from controls. Further investigations are required to study the possible implications of these changes and whether they can be used to monitor disease progression or determine the success of corneal collagen cross-linking.
Purpose:  To investigate the expression of proteases, proteolytic activity and cytokines in the tear film of people with keratoconus. Methods:  Basal tears from people with keratoconus, from individuals who had undergone corneal collagen cross‐linking for the treatment of keratoconus, and from normal controls were collected using a capillary tube. Corneal curvature of each subject was mapped. The total protein in tears was estimated. Levels and activity of proteases in the tears were analysed using specific antibody arrays and activity assays. Results:  The total tear protein level was significantly reduced in keratoconus (4.1 ± 0.9 mg/ml) compared with normals (6.7 ± 1.4 mg/ml) (p < 0.0001) or subjects who had undergone corneal collagen cross‐linking (5.7 ± 2.3 mg/ml) (p < 0.005). Significantly (p < 0.05) increased tear expression of matrix metalloproteinases (MMP) ‐1, ‐3, ‐7, ‐13, interleukins (IL) ‐4, ‐5, ‐6, ‐8 and tumour necrosis factor (TNF) ‐α, ‐β were evident in keratoconus. Tear IL‐6 was the only cytokine significantly (p < 0.05) increased in tears of keratoconus subjects compared with the collagen cross‐linked group. No significant difference in tear proteases were observed between the normal and the cross‐linked groups, although the expression of TNF‐α was significantly (p < 0.05) increased in the cross‐linked group compared with the controls. Elevated gelatinolytic (87.5 ± 33.6 versus 45.8 ± 24.6 FIU, p < 0.0001) and collagenolytic (6.1 ± 3.2 versus 3.6 ± 2.0 FIU, p < 0.05) activities were observed in tears from keratoconus compared with normal subjects. The activity of tear gelatinases (69.6 ± 22.2 FIU) and collagenases (5.7 ± 3.3 FIU) in the collagen cross‐linked group was not significantly different compared with either keratoconus or normals. Conclusion:  Tears of people with keratoconus had 1.9 times higher levels of proteolytic activity and over expression of several MMPs and cytokines compared with tears from controls. Further investigations are required to study the possible implications of these changes and whether they can be used to monitor disease progression or determine the success of corneal collagen cross‐linking.
Author Pye, David Cecil
Balasubramanian, Sivaraman Arumugam
Willcox, Mark Duncan Perry
Mohan, Sujatha
Author_xml – sequence: 1
  givenname: Sivaraman Arumugam
  surname: Balasubramanian
  fullname: Balasubramanian, Sivaraman Arumugam
  organization: Brien Holden Vision Institute, Sydney, NSW, Australia
– sequence: 2
  givenname: Sujatha
  surname: Mohan
  fullname: Mohan, Sujatha
  organization: Rajan Eye Care Hospitals, Chennai, Tamilnadu, India
– sequence: 3
  givenname: David Cecil
  surname: Pye
  fullname: Pye, David Cecil
  organization: School of Optometry and Vision Science, University of New South Wales, Sydney, NSW, Australia
– sequence: 4
  givenname: Mark Duncan Perry
  surname: Willcox
  fullname: Willcox, Mark Duncan Perry
  organization: Brien Holden Vision Institute, Sydney, NSW, Australia
BackLink https://www.ncbi.nlm.nih.gov/pubmed/22413749$$D View this record in MEDLINE/PubMed
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ContentType Journal Article
Copyright 2012 The Authors. Acta Ophthalmologica © 2012 Acta Ophthalmologica Scandinavica Foundation
2012 The Authors. Acta Ophthalmologica © 2012 Acta Ophthalmologica Scandinavica Foundation.
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References Fullard RJ & Snyder C (1990): Protein levels in nonstimulated and stimulated tears of normal human subjects. Invest Ophthalmol Vis Sci 31: 1119-1126.
Saghizadeh M, Brown DJ, Castellon R et al. (2001): Overexpression of matrix metalloproteinase-10 and matrix metalloproteinase-3 in human diabetic corneas: a possible mechanism of basement membrane and integrin alterations. Am J Pathol 158: 723-734.
Yoo HG, Shin BA, Park JS, Lee KH, Chay KO, Yang SY, Ahn BW & Jung YD (2002): IL-1beta induces MMP-9 via reactive oxygen species and NF-kappaB in murine macrophage RAW 264.7 cells. Biochem Biophys Res Commun 298: 251-256.
Fini ME, Yue BY & Sugar J (1992): Collagenolytic/gelatinolytic metalloproteinases in normal and keratoconus corneas. Curr Eye Res 11: 849-862.
Haro H, Crawford HC, Fingleton B, Shinomiya K, Spengler DM & Matrisian LM (2000): Matrix metalloproteinase-7-dependent release of tumor necrosis factor-alpha in a model of herniated disc resorption. J Clin Invest 105: 143-150.
Seppala HP, Maatta M, Rautia M, Mackiewicz Z, Tuisku I, Tervo T & Konttinen YT (2006): EMMPRIN and MMP-1 in keratoconus. Cornea 25: 325-330.
Sitaramamma T, Shivaji S & Rao GN (1998): HPLC analysis of closed, open, and reflex eye tear proteins. Indian J Ophthalmol 46: 239-245.
Jun AS, Cope L, Speck C, Feng X, Lee S, Meng H, Hamad A & Chakravarti S (2011): Subnormal cytokine profile in the tear fluid of keratoconus patients. PloS one 6: e16437.
Smith PK, Krohn RI, Hermanson GT et al. (1985): Measurement of protein using bicinchoninic acid. Anal Biochem 150: 76-85.
Sommer F, Fotzsch R, Pillunat LE & Wollensak G (2003): [Diagnostic and therapeutic problems in chronic progressive external ophthalmoplegia (CPEO)]. Klin Monatsbl Augenheilkd 220: 315-319.
Mazzotta C, Traversi C, Baiocchi S, Caporossi O, Bovone C, Sparano MC, Balestrazzi A & Caporossi A (2008): Corneal healing after riboflavin ultraviolet-A collagen cross-linking determined by confocal laser scanning microscopy in vivo: early and late modifications. Am J Ophthalmol 146: 527-533.
McMonnies CW (2007): Abnormal rubbing and keratectasia. Eye Contact Lens 33: 265-271.
Raiskup-Wolf F, Hoyer A, Spoerl E & Pillunat LE (2008): Collagen crosslinking with riboflavin and ultraviolet-A light in keratoconus: long-term results. Journal of cataract and refractive surgery 34: 796-801.
Rodriguez-Ausin P, Gutierrez-Ortega R, Arance-Gil A, Romero-Jimenez M & Fuentes-Paez G (2011): Keratopathy after cross-linking for keratoconus. Cornea 30: 1051-1053.
Fini ME, Cook JR & Mohan R (1998): Proteolytic mechanisms in corneal ulceration and repair. Arch Dermatol Res 290(Suppl): S12-S23.
Lema I & Duran JA (2005): Inflammatory molecules in the tears of patients with keratoconus. Ophthalmology 112: 654-659.
Shi GP, Munger JS, Meara JP, Rich DH & Chapman HA (1992): Molecular cloning and expression of human alveolar macrophage cathepsin S, an elastinolytic cysteine protease. J Biol Chem 267: 7258-7262.
Collier SA (2001): Is the corneal degradation in keratoconus caused by matrix-metalloproteinases? Clin Experiment Ophthalmol 29: 340-344.
Nakamura Y, Sotozono C & Kinoshita S (1998): Inflammatory cytokines in normal human tears. Curr Eye Res 17: 673-676.
Nakayasu K, Tanaka M, Konomi H & Hayashi T (1986): Distribution of types I, II, III, IV and V collagen in normal and keratoconus corneas. Ophthalmic Res 18: 1-10.
Ambrosio R Jr, Nogueira LP, Caldas DL, Fontes BM, Luz A, Cazal JO, Alves MR & Belin MW (2011): Evaluation of corneal shape and biomechanics before LASIK. Int Ophthalmol Clin 51: 11-38.
Ito A, Mukaiyama A, Itoh Y, Nagase H, Thogersen IB, Enghild JJ, Sasaguri Y & Mori Y (1996): Degradation of interleukin 1beta by matrix metalloproteinases. J Biol Chem 271: 14657-14660.
Kao WW, Vergnes JP, Ebert J, Sundar-Raj CV & Brown SI (1982): Increased collagenase and gelatinase activities in keratoconus. Biochem Biophys Res Commun 107: 929-936.
Taleb S, Lacasa D, Bastard JP et al. (2005): Cathepsin S, a novel biomarker of adiposity: relevance to atherogenesis. FASEB J 19: 1540-1542.
Ollivier FJ, Gilger BC, Barrie KP, Kallberg ME, Plummer CE, O'Reilly S, Gelatt KN & Brooks DE (2007): Proteinases of the cornea and preocular tear film. Vet Ophthalmol 10: 199-206.
Heinz A, Taddese S, Sippl W, Neubert RH & Schmelzer CE (2011): Insights into the degradation of human elastin by matrilysin-1. Biochimie 93: 187-194.
Pannebaker C, Chandler HL & Nichols JJ (2010): Tear proteomics in keratoconus. Mol vis 16: 1949-1957.
Li DQ, Shang TY, Kim HS, Solomon A, Lokeshwar BL & Pflugfelder SC (2003): Regulated expression of collagenases MMP-1, -8, and -13 and stromelysins MMP-3, -10, and -11 by human corneal epithelial cells. Invest Ophthalmol Vis Sci 44: 2928-2936.
Balasubramanian SA, Pye DC & Willcox MD (2010): Are proteinases the reason for keratoconus? Curr Eye Res 35: 185-191.
Labiris G, Kaloghianni E, Koukoula S, Zissimopoulos A & Kozobolis VP (2011): Corneal melting after collagen cross-linking for keratoconus: a case report. J Med Case Reports 5: 152.
Rehany U, Lahav M & Shoshan S (1982): Collagenolytic activity in keratoconus. Ann Ophthalmol 14: 751-754.
Koller T, Mrochen M & Seiler T (2009): Complication and failure rates after corneal crosslinking. J Cataract Refract Surg 35: 1358-1362.
Lema I, Sobrino T, Duran JA, Brea D & Diez-Feijoo E (2009): Subclinical keratoconus and inflammatory molecules from tears. Br J Ophthalmol 93: 820-824.
Sendide K, Deghmane AE, Pechkovsky D, Av-Gay Y, Talal A & Hmama Z (2005): Mycobacterium bovis BCG attenuates surface expression of mature class II molecules through IL-10-dependent inhibition of cathepsin S. J Immunol 175: 5324-5332.
Li DQ, Meller D, Liu Y & Tseng SC (2000): Overexpression of MMP-1 and MMP-3 by cultured conjunctivochalasis fibroblasts. Invest Ophthalmol Vis Sci 41: 404-410.
Uchio E, Ono SY, Ikezawa Z & Ohno S (2000): Tear levels of interferon-gamma, interleukin (IL) -2, IL-4 and IL-5 in patients with vernal keratoconjunctivitis, atopic keratoconjunctivitis and allergic conjunctivitis. Clin Exp Allergy 30: 103-109.
Alexander CM & Werb Z (1989): Proteinases and extracellular matrix remodeling. Curr Opin Cell Biol 1: 974-982.
Mackiewicz Z, Maatta M, Stenman M, Konttinen L, Tervo T & Konttinen YT (2006): Collagenolytic proteinases in keratoconus. Cornea 25: 603-610.
Leonardi A, Brun P, Abatangelo G, Plebani M & Secchi AG (2003): Tear levels and activity of matrix metalloproteinase (MMP)-1 and MMP-9 in vernal keratoconjunctivitis. Invest Ophthalmol Vis Sci 44: 3052-3058.
Maatta M, Kari O, Tervahartiala T et al. (2008): Elevated expression and activation of matrix metalloproteinase 8 in tear fluid in atopic blepharoconjunctivitis. Cornea 27: 297-301.
Fabre EJ, Bureau J, Pouliquen Y & Lorans G (1991): Binding sites for human interleukin 1 alpha, gamma interferon and tumor necrosis factor on cultured fibroblasts of normal cornea and keratoconus. Curr Eye Res 10: 585-592.
Kamma-Lorger CS, Boote C, Hayes S et al. (2010): Collagen and mature elastic fibre organisation as a function of depth in the human cornea and limbus. J Struct Biol 169: 424-430.
Wisithphrom K & Windsor LJ (2006): The effects of tumor necrosis factor-alpha, interleukin-1beta, interleukin-6, and transforming growth factor-beta1 on pulp fibroblast mediated collagen degradation. J Endod 32: 853-861.
Yoon KC, Jeong IY, Park YG & Yang SY (2007): Interleukin-6 and tumor necrosis factor-alpha levels in tears of patients with dry eye syndrome. Cornea 26: 431-437.
Brown D, Chwa MM, Opbroek A & Kenney MC (1993): Keratoconus corneas: increased gelatinolytic activity appears after modification of inhibitors. Curr Eye Res 12: 571-581.
Flanagan G & Binder PS (2003): Estimating residual stromal thickness before and after laser in situ keratomileusis. J Cataract Refract Surg 29: 1674-1683.
1990; 31
1982; 14
2010; 16
1989; 1
2010; 35
2005; 175
1991; 10
2005; 112
2006; 32
1982; 107
2010; 169
1992; 267
2000; 41
2002; 298
2011; 30
1986; 18
2008; 34
2001; 29
2008; 146
2007; 10
1992; 11
2011; 6
2007; 33
2011; 5
1998; 46
1998; 290
1993; 12
2009; 35
1998; 17
2005; 19
2000; 105
2009; 93
2011; 93
2011; 51
2008; 27
2006; 25
2000; 30
1996; 271
2003; 29
1985; 150
2001; 158
2003; 220
2003; 44
2007; 26
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References_xml – reference: Collier SA (2001): Is the corneal degradation in keratoconus caused by matrix-metalloproteinases? Clin Experiment Ophthalmol 29: 340-344.
– reference: Raiskup-Wolf F, Hoyer A, Spoerl E & Pillunat LE (2008): Collagen crosslinking with riboflavin and ultraviolet-A light in keratoconus: long-term results. Journal of cataract and refractive surgery 34: 796-801.
– reference: Mackiewicz Z, Maatta M, Stenman M, Konttinen L, Tervo T & Konttinen YT (2006): Collagenolytic proteinases in keratoconus. Cornea 25: 603-610.
– reference: Saghizadeh M, Brown DJ, Castellon R et al. (2001): Overexpression of matrix metalloproteinase-10 and matrix metalloproteinase-3 in human diabetic corneas: a possible mechanism of basement membrane and integrin alterations. Am J Pathol 158: 723-734.
– reference: Nakamura Y, Sotozono C & Kinoshita S (1998): Inflammatory cytokines in normal human tears. Curr Eye Res 17: 673-676.
– reference: Nakayasu K, Tanaka M, Konomi H & Hayashi T (1986): Distribution of types I, II, III, IV and V collagen in normal and keratoconus corneas. Ophthalmic Res 18: 1-10.
– reference: Kao WW, Vergnes JP, Ebert J, Sundar-Raj CV & Brown SI (1982): Increased collagenase and gelatinase activities in keratoconus. Biochem Biophys Res Commun 107: 929-936.
– reference: Li DQ, Meller D, Liu Y & Tseng SC (2000): Overexpression of MMP-1 and MMP-3 by cultured conjunctivochalasis fibroblasts. Invest Ophthalmol Vis Sci 41: 404-410.
– reference: Jun AS, Cope L, Speck C, Feng X, Lee S, Meng H, Hamad A & Chakravarti S (2011): Subnormal cytokine profile in the tear fluid of keratoconus patients. PloS one 6: e16437.
– reference: Sommer F, Fotzsch R, Pillunat LE & Wollensak G (2003): [Diagnostic and therapeutic problems in chronic progressive external ophthalmoplegia (CPEO)]. Klin Monatsbl Augenheilkd 220: 315-319.
– reference: Ambrosio R Jr, Nogueira LP, Caldas DL, Fontes BM, Luz A, Cazal JO, Alves MR & Belin MW (2011): Evaluation of corneal shape and biomechanics before LASIK. Int Ophthalmol Clin 51: 11-38.
– reference: Smith PK, Krohn RI, Hermanson GT et al. (1985): Measurement of protein using bicinchoninic acid. Anal Biochem 150: 76-85.
– reference: Taleb S, Lacasa D, Bastard JP et al. (2005): Cathepsin S, a novel biomarker of adiposity: relevance to atherogenesis. FASEB J 19: 1540-1542.
– reference: Mazzotta C, Traversi C, Baiocchi S, Caporossi O, Bovone C, Sparano MC, Balestrazzi A & Caporossi A (2008): Corneal healing after riboflavin ultraviolet-A collagen cross-linking determined by confocal laser scanning microscopy in vivo: early and late modifications. Am J Ophthalmol 146: 527-533.
– reference: Leonardi A, Brun P, Abatangelo G, Plebani M & Secchi AG (2003): Tear levels and activity of matrix metalloproteinase (MMP)-1 and MMP-9 in vernal keratoconjunctivitis. Invest Ophthalmol Vis Sci 44: 3052-3058.
– reference: Balasubramanian SA, Pye DC & Willcox MD (2010): Are proteinases the reason for keratoconus? Curr Eye Res 35: 185-191.
– reference: Seppala HP, Maatta M, Rautia M, Mackiewicz Z, Tuisku I, Tervo T & Konttinen YT (2006): EMMPRIN and MMP-1 in keratoconus. Cornea 25: 325-330.
– reference: Fabre EJ, Bureau J, Pouliquen Y & Lorans G (1991): Binding sites for human interleukin 1 alpha, gamma interferon and tumor necrosis factor on cultured fibroblasts of normal cornea and keratoconus. Curr Eye Res 10: 585-592.
– reference: Flanagan G & Binder PS (2003): Estimating residual stromal thickness before and after laser in situ keratomileusis. J Cataract Refract Surg 29: 1674-1683.
– reference: Haro H, Crawford HC, Fingleton B, Shinomiya K, Spengler DM & Matrisian LM (2000): Matrix metalloproteinase-7-dependent release of tumor necrosis factor-alpha in a model of herniated disc resorption. J Clin Invest 105: 143-150.
– reference: Lema I & Duran JA (2005): Inflammatory molecules in the tears of patients with keratoconus. Ophthalmology 112: 654-659.
– reference: Fini ME, Cook JR & Mohan R (1998): Proteolytic mechanisms in corneal ulceration and repair. Arch Dermatol Res 290(Suppl): S12-S23.
– reference: Ito A, Mukaiyama A, Itoh Y, Nagase H, Thogersen IB, Enghild JJ, Sasaguri Y & Mori Y (1996): Degradation of interleukin 1beta by matrix metalloproteinases. J Biol Chem 271: 14657-14660.
– reference: Ollivier FJ, Gilger BC, Barrie KP, Kallberg ME, Plummer CE, O'Reilly S, Gelatt KN & Brooks DE (2007): Proteinases of the cornea and preocular tear film. Vet Ophthalmol 10: 199-206.
– reference: Alexander CM & Werb Z (1989): Proteinases and extracellular matrix remodeling. Curr Opin Cell Biol 1: 974-982.
– reference: Fullard RJ & Snyder C (1990): Protein levels in nonstimulated and stimulated tears of normal human subjects. Invest Ophthalmol Vis Sci 31: 1119-1126.
– reference: McMonnies CW (2007): Abnormal rubbing and keratectasia. Eye Contact Lens 33: 265-271.
– reference: Heinz A, Taddese S, Sippl W, Neubert RH & Schmelzer CE (2011): Insights into the degradation of human elastin by matrilysin-1. Biochimie 93: 187-194.
– reference: Lema I, Sobrino T, Duran JA, Brea D & Diez-Feijoo E (2009): Subclinical keratoconus and inflammatory molecules from tears. Br J Ophthalmol 93: 820-824.
– reference: Shi GP, Munger JS, Meara JP, Rich DH & Chapman HA (1992): Molecular cloning and expression of human alveolar macrophage cathepsin S, an elastinolytic cysteine protease. J Biol Chem 267: 7258-7262.
– reference: Wisithphrom K & Windsor LJ (2006): The effects of tumor necrosis factor-alpha, interleukin-1beta, interleukin-6, and transforming growth factor-beta1 on pulp fibroblast mediated collagen degradation. J Endod 32: 853-861.
– reference: Rehany U, Lahav M & Shoshan S (1982): Collagenolytic activity in keratoconus. Ann Ophthalmol 14: 751-754.
– reference: Yoo HG, Shin BA, Park JS, Lee KH, Chay KO, Yang SY, Ahn BW & Jung YD (2002): IL-1beta induces MMP-9 via reactive oxygen species and NF-kappaB in murine macrophage RAW 264.7 cells. Biochem Biophys Res Commun 298: 251-256.
– reference: Sitaramamma T, Shivaji S & Rao GN (1998): HPLC analysis of closed, open, and reflex eye tear proteins. Indian J Ophthalmol 46: 239-245.
– reference: Koller T, Mrochen M & Seiler T (2009): Complication and failure rates after corneal crosslinking. J Cataract Refract Surg 35: 1358-1362.
– reference: Sendide K, Deghmane AE, Pechkovsky D, Av-Gay Y, Talal A & Hmama Z (2005): Mycobacterium bovis BCG attenuates surface expression of mature class II molecules through IL-10-dependent inhibition of cathepsin S. J Immunol 175: 5324-5332.
– reference: Uchio E, Ono SY, Ikezawa Z & Ohno S (2000): Tear levels of interferon-gamma, interleukin (IL) -2, IL-4 and IL-5 in patients with vernal keratoconjunctivitis, atopic keratoconjunctivitis and allergic conjunctivitis. Clin Exp Allergy 30: 103-109.
– reference: Brown D, Chwa MM, Opbroek A & Kenney MC (1993): Keratoconus corneas: increased gelatinolytic activity appears after modification of inhibitors. Curr Eye Res 12: 571-581.
– reference: Maatta M, Kari O, Tervahartiala T et al. (2008): Elevated expression and activation of matrix metalloproteinase 8 in tear fluid in atopic blepharoconjunctivitis. Cornea 27: 297-301.
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Snippet . Purpose:  To investigate the expression of proteases, proteolytic activity and cytokines in the tear film of people with keratoconus. Methods:  Basal tears...
Purpose:  To investigate the expression of proteases, proteolytic activity and cytokines in the tear film of people with keratoconus. Methods:  Basal tears...
To investigate the expression of proteases, proteolytic activity and cytokines in the tear film of people with keratoconus. Basal tears from people with...
To investigate the expression of proteases, proteolytic activity and cytokines in the tear film of people with keratoconus.PURPOSETo investigate the expression...
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SubjectTerms Adult
Collagen - metabolism
Collagenases - metabolism
Corneal Stroma - metabolism
Corneal Topography
Cross-Linking Reagents - therapeutic use
cytokines
Cytokines - metabolism
Eye Proteins - metabolism
Female
Gelatinases - metabolism
Humans
keratoconus
Keratoconus - drug therapy
Keratoconus - metabolism
Male
Peptide Hydrolases - metabolism
Photosensitizing Agents - therapeutic use
proteases
Proteolysis
Riboflavin - therapeutic use
tears
Tears - metabolism
Title Proteases, proteolysis and inflammatory molecules in the tears of people with keratoconus
URI https://api.istex.fr/ark:/67375/WNG-CLNKLVJ1-F/fulltext.pdf
https://onlinelibrary.wiley.com/doi/abs/10.1111%2Fj.1755-3768.2011.02369.x
https://www.ncbi.nlm.nih.gov/pubmed/22413749
https://www.proquest.com/docview/1017758893
Volume 90
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